A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082481



Internal ID21991714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60274666..60274666hg38UCSC Ensembl
chr14:60741384..60741384hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601395
Samples
Known GenesPPM1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082481
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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